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Deviation Investigation Technical Writer

Job in Concord, Cabarrus County, North Carolina, 28027, USA
Listing for: Medasource
Full Time position
Listed on 2025-12-23
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Deviation Investigation Technical Writer Location

Concord, North Carolina

Position Description

The Client is seeking a detail-oriented and technically proficient Deviation Investigator to support deviation investigations and technical report writing. This role is responsible for investigating and documenting deviations and non-conformances, ensuring clear, thorough, and compliant documentation. The ideal candidate has strong analytical and writing skills, attention to detail, and the ability to evaluate complex technical issues with precision.

Responsibilities
  • Conduct thorough investigations into deviations, identifying root causes and contributing factors
  • Write clear, concise, and technically accurate deviation investigation reports
  • Collaborate with cross-functional teams to gather required information and ensure timely resolution of deviations
  • Apply critical thinking and technical knowledge to assess issues and recommend corrective and preventive actions (CAPAs)
  • Ensure compliance with internal procedures and applicable regulatory requirements
Requirements
  • Proven ability to write technical documentation or investigation reports
  • Strong analytical skills and attention to detail
  • Ability to assess and interpret technical or process-related issues
  • Excellent written and verbal communication skills
  • Proficiency with Microsoft Office Suite or similar tools
Preferred Qualifications
  • Background in a technical field such as engineering, life sciences, or quality assurance
  • Experience in pharmaceutical or biotechnology industries
  • Familiarity with manufacturing environments and processes
  • Understanding of deviation management systems and CAPA processes
  • Ability to work independently and manage multiple priorities
Additional Information
  • Training and support will be provided to ensure success in the role
  • Candidates without direct pharmaceutical or manufacturing experience are encouraged to apply if core requirements are met
  • This position offers a dynamic work environment with opportunities to contribute to continuous improvement initiatives
Seniority Level

Associate

Employment Type

Full-time

Job Function

Writing/Editing

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care

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